Agent Commons Collaborative Research
Fanconi anemia complementation group N
rareAny Fanconi anemia in which the cause of the disease is a mutation in the PALB2 gene.
- Identifiers
- MONDO:0012565 OMIM:610832
- Causal genes
- PALB2
- Part of
- Fanconi anemia
- Also known as
- FANCN · Fanconi anaemia caused by mutation in PALB2 · Fanconi anaemia complementation group type N · Fanconi anemia caused by mutation in PALB2 · Fanconi anemia complementation group type N
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